A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705498



Internal ID15442150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119779396..119791100hg38UCSC Ensembl
Innerchr11:119650105..119661809hg19UCSC Ensembl
Innerchr11:119155315..119167019hg18UCSC Ensembl
Innerchr11:119155315..119167019hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3811705
hg1911705
hg1811705
hg1711705
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528824
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705498
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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